Canonical Allele Identifier: CA2038228919
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041587T= , CM000674.2:g.56041587T= GRCh38
NC_000012.11:g.56435371T= , CM000674.1:g.56435371T= GRCh37
NC_000012.10:g.54721638T= NCBI36
NG_023201.1:g.4686T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+191T= ENSP00000348849.5:n.-357+191T=
XR_944989.1:n.126A=
XR_944990.1:n.126A=
XR_944989.3:n.417A=
XR_944990.3:n.417A=